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Quality Assurance Analyst
2 months ago
Company: SRG
Type: Permanent Position
Salary: Competitive Package
SRG is pleased to assist a clinical trial manufacturer in their search for a Quality Assurance Specialist. As the company continues to grow, they are seeking two professionals in the field of sterile manufacturing.
Key Responsibilities:
- Engage with stakeholders to ensure the effective management and timely completion of quality assurance tasks.
- Handle deviations, conduct investigations, and implement corrective actions.
- Supervise the documentation process, including the review and approval of standard operating procedures, batch records, and other controlled documents.
- Ensure proper management of the document lifecycle, maintaining compliance with regulatory standards and industry best practices.
- Assess site compliance and drive enhancements through internal audits.
Requirements:
- Proven experience in quality assurance within a pharmaceutical environment.
- Familiarity with process validation and cleaning validation and verification.
- Experience in a sterile manufacturing setting is preferred.
- Expertise in managing validation lifecycles from inception to retirement.
- Strong knowledge of equipment, facility, and process change management.
- Excellent communication skills, both written and verbal, along with computer proficiency.
- Ability to prioritize tasks, manage workload effectively, and meet deadlines.
- Strong attention to detail and commitment to high-quality work output.
This role presents an exciting opportunity for a dynamic and motivated professional to contribute to a growing company while enhancing their career with valuable skills.
